Inhibitory Effects of Dicaffeoylquinic Acids from Artemisia dubia on Aldo-keto Reductase Family 1B10

Authors
Lee, Hee JuLee, Joo YoungKim, Sang MinNho, Chu WonJung, Sang HoonSong, Dae-GeunKim, Chul YoungPan, Cheol-Ho
Issue Date
2010-12
Publisher
KOREAN SOC APPLIED BIOLOGICAL CHEMISTRY
Citation
JOURNAL OF THE KOREAN SOCIETY FOR APPLIED BIOLOGICAL CHEMISTRY, v.53, no.6, pp.826 - 830
Abstract
The ethyl acetate fraction of Artemisia dubia showed a potent inhibitory activity on recombinant human AKR1B10 (rh AKR1B10). Due to its potency, subsequent purification of ethyl acetate fraction led to seven compounds including five dicaffeoylquinic acid (DCQA) derivatives. Compounds were identified as 3,4-dihydroxybenzoic acid (1), quercetin 3-O-beta-glucose (2), 3,4-DCQA (3), 3,5-DCQA (4), 4,5-DCQA (5), 3,5-DCQA methyl ester (6), and 4,5-DCQA methyl ester (7). A series of DCQA derivatives (3-7) showed inhibitory activity on rhAKR1B10 in the range of IC50 1.24-2.29 1. mu M, whereas 3,4-dihydroxybenzoic acid and quercetin 3-O-beta-glucose showed no inhibitory activity on rhAKR1B10.
Keywords
CANCER-CELLS; BREAST-CANCER; B10; AKR1B10; GENE; IDENTIFICATION; DERIVATIVES; CARCINOMAS; LIVER; CANCER-CELLS; BREAST-CANCER; B10; AKR1B10; GENE; IDENTIFICATION; DERIVATIVES; CARCINOMAS; LIVER; AKR1B10; aldose reductase-like; anticancer; DCQA; dicaffeoylquinic acid; Artemisia dubia
ISSN
1738-2203
URI
https://pubs.kist.re.kr/handle/201004/130872
DOI
10.3839/jksabc.2010.125
Appears in Collections:
KIST Article > 2010
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